{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Marlborough",
      "state": "MA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90458",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "100 Boston Scientific Way",
      "address_2": "N/A",
      "postal_code": "01752-1234",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution to AR CA IL ME MI NC TX Foreign distribution to Australia, Canada, and France.",
      "recall_number": "Z-1392-2022",
      "product_description": "GreenLight HPSEA Laser Fibers, UPN 0010-2092",
      "product_quantity": "57",
      "reason_for_recall": "Several complaints were received for the affected lot; users received a \"Fiber type does not match card type\" error message on the GreenLight XPS Laser console, necessitating the replacement of the laser fiber and fiber card. This may result in prolonged procedure while the fiber is being replaced.",
      "recall_initiation_date": "20220531",
      "center_classification_date": "20220715",
      "report_date": "20220727",
      "code_info": "UDI-DI (GTIN): 00878953005522 Lot: 27770466"
    }
  ]
}